C-X-C Motif Chemokine Receptor 4-Directed Scintigraphy Using [99mTc]Tc-Pentixatec in Primary Aldosteronism: A Proof-of-Concept Study

J Nucl Med. 2024 Oct 1;65(10):1640-1644. doi: 10.2967/jnumed.124.268169.

Abstract

C-X-C motif chemokine receptor 4 (CXCR4)-directed imaging has gained clinical interest in aiding clinical diagnostics in primary aldosteronism (PA). We retrospectively evaluated the feasibility of CXCR4-directed scintigraphy using the novel CXCR-4 ligand [99mTc]Tc-pentixatec in patients with PA. Methods: Six patients (mean age ± SD, 49 ± 15 y) underwent CXCR4-directed scintigraphy (including planar imaging and SPECT/CT) 30, 120, and 240 min after injection of 435 ± 50 MBq of [99mTc]Tc-pentixatec. Adrenal CXCR4 expression was analyzed by calculating lesion-to-contralateral ratios (LCRs). Imaging results were correlated to clinical information. Histopathology and clinical follow-up served as the standard of reference. Results: Three subjects showed lateralization of adrenal tracer accumulation, with a mean maximum lesion-to-contralateral ratio of 1.65 (range, 1.52-1.70), which correlated with morphologic findings on CT. One individual underwent adrenalectomy and presented with complete biochemical and clinical remission at follow-up. Histopathologic workup confirmed unilateral aldosterone-producing adenoma. Conclusion: [99mTc]Tc-pentixatec scintigraphy with SPECT in patients with PA is feasible and might offer a valuable alternative to CXCR4-directed imaging with [68Ga]Ga-pentixafor PET.

Keywords: CXCR4-directed imaging; primary aldosteronism; scintigraphy.

MeSH terms

  • Adrenal Glands / diagnostic imaging
  • Adult
  • Aged
  • Female
  • Humans
  • Hyperaldosteronism* / diagnostic imaging
  • Male
  • Middle Aged
  • Organotechnetium Compounds*
  • Proof of Concept Study
  • Radiopharmaceuticals
  • Receptors, CXCR4* / metabolism
  • Retrospective Studies
  • Single Photon Emission Computed Tomography Computed Tomography

Substances

  • Receptors, CXCR4
  • Organotechnetium Compounds
  • CXCR4 protein, human
  • Radiopharmaceuticals